# Main branches pulmonary artery stenting in congenital heart diseases: a case series

**Authors:** Radityo Prakoso, Yovi Kurniawati, Sisca Natalia Siagian, Aditya Agita Sembiring, Damba Dwisepto Aulia Sakti, Brian Mendel, Olfi Lelya, Oktavia Lilyasari

PMC · DOI: 10.3389/fcvm.2026.1732330 · Frontiers in Cardiovascular Medicine · 2026-03-04

## TL;DR

Pulmonary artery stenting is a safe and effective treatment for branch stenosis in children with complex heart defects, improving oxygen levels and reducing complications.

## Contribution

This study presents a case series demonstrating the safety and efficacy of pulmonary artery stenting in pediatric patients with congenital heart disease.

## Key findings

- PA stenting improved oxygen saturation from 78.1% to 91.6% in patients with branch PA stenosis.
- Procedural success was achieved in all 18 cases, with complications occurring in only five instances.
- Most surviving patients showed sustained improvement and progressed to definitive surgical repair.

## Abstract

Branch pulmonary artery (PA) stenosis is a common complication in congenital heart disease (CHD) that can result in unequal pulmonary perfusion, cyanosis, and increased ventricular workload. Although surgical repair remains an option, pulmonary artery stenting has emerged as a less invasive and effective alternative for restoring vessel patency.

This single-center retrospective study included 18 pediatric patients (median age 5.4 years, range 3 months–17 years) who underwent PA stenting for branch stenosis associated with complex CHD. Patient demographics, procedural characteristics, complications, and follow-up outcomes were analyzed.

A total of 19 stents were successfully implanted; 10 in the left PA, 7 in the right PA, and one case of bilateral stenting. The mean pre-procedural oxygen saturation improved from 78.1% ± 12.5 to 91.6% ± 7.3 during follow-up. Procedural success was achieved in all cases. Five complications were recorded, including one case of stent dislodgement requiring surgical retrieval and one case of inadequate stent expansion due to over-compliant pulmonary arteries. Three deaths occurred, all attributed to underlying clinical deterioration rather than the procedure itself. No instances of vascular rupture or pericardial tamponade were observed. Most surviving patients demonstrated sustained improvement in oxygenation and progressed to definitive surgical repair or Fontan completion.

Pulmonary artery stenting is a safe and effective intervention for managing branch PA stenosis in complex pediatric CHD, providing significant hemodynamic and clinical benefits with an acceptable complication profile. Careful pre-procedural imaging, appropriate stent selection, and meticulous deployment technique are essential to prevent complications such as dislodgement or incomplete expansion, ensuring durable long-term outcomes.

## Linked entities

- **Diseases:** congenital heart disease (MONDO:0005453)

## Full-text entities

- **Diseases:** Branch pulmonary artery (PA) stenosis (MESH:D000071079), deaths (MESH:D003643), branch stenosis (MESH:D003251), vascular rupture (MESH:D012421), cyanosis (MESH:D003490), pericardial tamponade (MESH:D002305), CHD (MESH:D006330)
- **Chemicals:** oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12996121/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996121/full.md

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Source: https://tomesphere.com/paper/PMC12996121